Curcumin

製品コードS1848 バッチS184803

印刷

化学情報

 Chemical Structure Synonyms Diferuloylmethane, Natural Yellow 3, Turmeric yellow Storage
(From the date of receipt)
3 years -20°C powder
1 years -80°C in solvent
化学式

C21H20O6

分子量 368.38 CAS No. 458-37-7
Solubility (25°C)* 体外 DMSO 74 mg/mL (200.87 mM)
Water Insoluble
Ethanol Insoluble
体内 (毎回新しく調製した物を用意してください)
Homogeneous suspension
CMC-NA
≥5mg/ml Taking the 1 mL working solution as an example, add 5 mg of this product to 1 ml of CMC-Na solution, mix evenly to obtain a homogeneous suspension with a final concentration of 5 mg/ml.
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液(一定の濃度)を調合する

生物活性

製品説明 Curcumin (Diferuloylmethane, Natural Yellow 3, Turmeric yellow) is the principal curcuminoid of the popular Indian spice turmeric, which is a member of the ginger family (Zingiberaceae). It is an inhibitor of p300 histone acetylatransferase(IC50~25 μM)and Histone deacetylase (HDAC); activates Nrf2 pathway and supresses the activation of NF-κB. Curcumin induces mitophagy, autophagy, apoptosis, and cell cycle arrest with antitumor activity. Curcumin reduces renal damage associated with rhabdomyolysis by decreasing ferroptosis-mediated cell death. Curcumin exhibits anti-infective properties against various human pathogens like the influenza virus, hepatitis C virus, HIV and so on.
in vitro

Curcumin induces the expression of forkhead box protein O1 (FOXO1) through activation of extracellular signal-regulated kinase 1/2 signaling. This compound inhibits cell proliferation, which was associated with upregulation of the cyclin-dependent kinase inhibitors, p27 and p21, and downregulation of cyclin D1[2]. It induces endoplasmic reticulum (ER) stress and mitochondrial dysfunction as evidenced by up-regulation of CCAAT/enhancer binding protein homologous protein (CHOP), phosphorylation of JNK and down-regulation of SERCA2ATPase, release of cytochrome c, decrease of Bcl-2 and reduction of mitochondrial membrane potential in both AGS and HT-29 cells[3].

in vivo

Chronic treatment with curcumin significantly reverses the CMS-induced behavioral abnormalities in stressed rats. Additionally, this compound effectively inhibits cytokine gene expression at both the mRNA and the protein level and reduces the activation of NF-κB[4].

プロトコル(参考用のみ)

細胞アッセイ 細胞株 murine melanoma cell subline(B16-R)
濃度 0-100 μM
反応時間 24-48 h
実験の流れ

1×104 B16-R cells are cultivated as monolayer culture for 12 hr. They were then incubated in 200 μL of RPMI, 10% FBS containing curcumin at final concentrations from 1–100 μM in 96-multiwell plates for 24-48 hr. After these incubations, cells are washed twice in PBS and 500 μl of fresh culture medium containing MTT (0.3 mg/mL) are added for colorimetric assay.

動物実験 動物モデル Female B6D2F1 mice (6-8 weeks old)
投薬量 25 mg/kg
投与方法 i.p.

参考

  • https://pubmed.ncbi.nlm.nih.gov/23871787/
  • https://pubmed.ncbi.nlm.nih.gov/23886126/
  • https://pubmed.ncbi.nlm.nih.gov/23881281/
  • https://pubmed.ncbi.nlm.nih.gov/23876788/
  • https://pubmed.ncbi.nlm.nih.gov/15221965/
  • https://pubmed.ncbi.nlm.nih.gov/15383533/
  • https://pubmed.ncbi.nlm.nih.gov/17927689/
  • https://pubmed.ncbi.nlm.nih.gov/7559628/
  • https://pubmed.ncbi.nlm.nih.gov/31034781/

カスタマーフィードバック

Data from [Oncol Res, 2014, 21(3), 137-44]

Data from [Oncol Res, 2014, 21(3), 137-44]

Data from [Data independently produced by , , J Exp Clin Cancer Res, 2018, 37(1):303]

Selleckの高級品が、幾つかの出版された研究調査結果(以下を含む)で使われた:

Calcium triggers calmodulin degradation to induce EGF receptor instability and overcome non-small cell lung cancer resistance to tyrosine kinase inhibitors [ J Biol Chem, 2025, 301(7):110305] PubMed: 40447190
Curcumin relieves CFA-induced inflammatory pain by inhibiting the AP-1/c-Jun-CCL2-CCR2 pathway in the spinal dorsal horn [ Mol Pain, 2025, 21:17448069251323668] PubMed: 39950445
Curcumin blunts epithelial-mesenchymal transition to alleviate invasion and metastasis of prostate cancer through the JARID1D demethylation [ Cancer Cell Int, 2024, 24(1):303] PubMed: 39218854
Patient-derived rhabdomyosarcoma cells recapitulate the genetic and transcriptomic landscapes of primary tumors [ iScience, 2024, 27(10):110862] PubMed: 39319271
Network-based prediction of anti-cancer drug combinations [ Front Pharmacol, 2024, 15:1418902] PubMed: 39211773
Schistosomicidal effects of histone acetyltransferase inhibitors against Schistosoma japonicum juveniles and adult worms in vitro [ PLoS Negl Trop Dis, 2024, 18(8):e0012428] PubMed: 39159234
The Cytotoxic Effect of Curcumin in Rhabdomyosarcoma Is Associated with the Modulation of AMPK, AKT/mTOR, STAT, and p53 Signaling [ Nutrients, 2023, 15(3)740] PubMed: 36771452
Curcumin suppress inflammatory response in traumatic brain injury via p38/MAPK signaling pathway [ Phytother Res, 2022, 36(3):1326-1337] PubMed: 35080289
MicroRNA profiling of paediatric AML with FLT-ITD or MLL-rearrangements: Expression signatures and in vitro modulation of miR-221-3p and miR-222-3p with BRD4/HATs inhibitors [ Oncol Rep, 2022, 48(6)221] PubMed: 36321792
Curcumin assists anti-EV71 activity of IFN-α by inhibiting IFNAR1 reduction in SH-SY5Y cells [ Gut Pathog, 2022, 14(1):8] PubMed: 35151347

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

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